Canonical Allele Identifier: PA916028368
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 210480
ClinVar RCV Id: RCV000194327 RCV002503752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ile377Val
CA208433
NM_001330579.2:c.1129A>G